21R0 to Have Iengthened Because the Ratio of Mg2+:Al3+ in the Starting Ma

Total Page:16

File Type:pdf, Size:1020Kb

21R0 to Have Iengthened Because the Ratio of Mg2+:Al3+ in the Starting Ma 21r0 MINIiRALOGICAL NOTIiS to have Iengthenedbecause the ratio of Mg2+:Al3+in the starting ma- terials was greaterthan the ratio of 7 :3" Brucite was presentin Run V-9 and boehmite was present in Run \,'-10; from this it seemsthat the range of the solid solution of Mgz+ and Al3+ in the hydroxide layer is limited. Valleriite was not produced at the temperatureof 700"C in any of the runs, and valleriite was also not produced at the temperature of 650'C in Run V-3. From this fact, the upper stable temperature of this minerai appearsto be between600oC and 650oC. Rolnnrxcrs Evexs, H. T., Mrr,rox, C., Cn.ro, E. C. T., Arr-rr, L, Mnln, C., INcnau, B., eNl Brnmn, R. A. (1964) Valleriite and the neu' iron sulfide, mackinawite, U. S. Geol,.Stut. Pro.f. Pap. 475'D, 64-69. -, AND Ar.r-umw, R (1968) The cr5'5111structure and cr1'stal chemistry of valleriite, Z. Kristallo gr., 127, 73-93. Senrmcnt, G. (1968) Electronprobe analyses of mackinarvite and valleriite, Neues Jahrb. M iner al. M onatsh. 8, 252-258. 'fut:rr,n, 9. p. (1949) Two pressure vesselsfor silicate-rvater systems, Geol. Soc.Amer. Buli. 60. 1727,1729 TIIE AMERICAN I{INERALOGIST, \IOL 55, NOVEMBDR-DECEMBER, 1970 A "VALLERIITE-TYI)E" X{INERAL FRO\{ NORIL'SK, WESTERN SIBERIAI D. C. Hanus, L. J. Cenu, J. M. Srowanr, Mineral' Sciences Diaision, Mines Branch, Ottazua. Alstnecr Electron microprobe analysis of a "valleriite-type" mineral from Noril'sk, western Siberia, yields a formula (CuoggsFerooaSz).1.472 [Fe(OH)z], u'hich is the most iron-rich variant of this mineral reported to date. INrnotucrtox The structure of valleriite from Loolekop, South Africa, determined very recently by Evans and AIImann (1968), has been interpreted as Iayers of copper-iron sulphide alternating with layers of Mg-AI hydrox- ide. The formula for the Loolekop material is (Fe1.q7Cu6.e3Sr) '1.526[MBo.e sAlo rr(OH) r]. Springer (1968) re-examined valleriites from two localities: Kaveltorp, Swedenand Palabora, South Africa with the electron microprobe an- l Sulphide Research Contribution No. 20, Mineral SciencesDivision. M TN ].R-4LOGI C A L,!\ OT] iS Frc. 1. Photomicrograph showing the oriented "valleriite" inclusions (5) in a cubanite lath (3), set in a matrix of talnakhite (1). The surface of the "valleriite" varies from smooth to rough. alyzer.This work showedthat the Palaboramaterial is the ordinary Mg- and Al-containing valleriite, whereas the Kaveltorp samples contain more iron than can be accountedfor by the sulphide sublattice. This suggeststhat there must be someiron in the hydroxide lattice replacing aluminum or magnesium.The formula derived for the Kaveltorp miner- al is (Cus.s1Fe1.1eSz). 1.56[M96 33Fe6 s7(OH)2]. In addition to the ordinary valleriite at Palabora,there is alsoanother variety of this mineral, which occurs in the magnetite-apatite-olivine rock of that district. This valleriite contains more iron and lessaluminum than the ordinary valleriite, and gives a formula (Cu1.saFes.e6Sr)'1.67 [M go.zbAIo.osFeo.ro(OH)z]. Valleriite from Noril'sk, western Siberia, has been reported inde- pendently by Genkin and Vyal'sov (1967), Cabri and Traill (1966), and Cabri (1967). Genkin and Vyal'sov reported on valleriite and mack- inawite, and gave X-ray powder data and optical and heating properties for valleriite, including X-ray powder data for the Noril'sk "valleriite." 2ll) I'IINI:.1<ALO(]|C\L NOT'liS Talr-n 1. X-R.q,v Powoen Dmln,rcrrolc D,rra lon "VAr-LBRrrrE-TvpE" Mrrtrnar. lrou Nonrr,'sr, WBsrrnw Srlpnre This St LdVyal'sov (1967) a:3.778+ Noril'sk c:34.747+ .O1 (2) (3) d(calc)A d(meas;A 1(est) d(meas)A 1(est) d(meas)A t1 nt 11382 9 11.38 3 + I I .JO 2 7.24" 00.6 .5.691 l0 .5.69 10 5.65 l0 5.71 00.9 3.794 8 3 .788 5 J.lt 5 3.81 10.1 3.257 9 3.259 o 3.28 9 3.27 lnt 3.214 4 324 i 321 2 3.1+6" 10.4 3 055 o 3 .049b 4 3 .03 10.5 2.951 I 2 952 00.12 2.846 2 2.845 1 2.85 2.79 z 2.770" 1 2.77 l0.7 2.7li- 2 2 674" 10.8 2.597 1 2.592 4 2 486" 3 248 J 2.51 10.10 2.363 1 2.359 3 2.36 00.15 ' JJJ) 2.269 3 227 3 228 10 TI 2.252( o J 2.142" 5 2.14 10.13 2.048 J 2.049 10.14 1.956 1 1 958 00.18 1.8e71 1.897 6 1.902 7 1 911 11.0 1.889i 7 11.3 1.864 7 9 t .864 2 r.877 11.6 1.793\ 10 16 1.788 I 10.T7 1.712.i 11.9 r.692f 1.692 20.1 1.6341 20.2 1.6291 1 630 t OJJ 1.633 00.27 1.626) 20.4 1.609r, 205 1 <Ot/ .5 1 600 I ..598 1 .599 10 19 1.57s1 t.577b 2 tl 12 1..574 | 20.7 1.ss1J 20.I4 1.175 1.416 114.6 mm dia. Debve-Scherrer Camera. Fe-l'iltered Co Tladiation Spacegroup R3rir (Evans a;d Allmann, 1968). 'Extra reflections. r, Talnakhite reflections. (2) Vein formation in "cubic chalcopyrite". (3) ltine-grained lamellar crvstals of valleriite from a cavity in "cubic chalcopyrite". Cabri's identification was based on an X-ray powder pattern using a .i7.3-mm-diameter Debve-Scherrercamera, and the similarity of its optical propertiesto those of other valleriites.He was not certain of the identitv of similar finer grained rnaterial which occurs as replacements MINER-ALOGICAL NOTES 2rt3 within cubanite lamellaeand reported this also as valleriite or mackina- wite; hence,a restudy of this material was undertaken. For a description of the copper-nickelores of the Talnakh deposit, Noril'sk, the readeris referredto a recent paper by Genkin el al. (1969). Ttto t'VelrBRrrrE-TYPE" MtNBner Electron microprobe analyseswere macieof the Noril'sk "valleriite" in a vuggl- sample kindly supplied by the Leningrad Mining Museum and labelledas "cubic chalcopyrite." Analysesof inclusionsin cubanite (Figure 1) and of larger areasof "valleriite" that had previously been X rayed, gave an averagecomposition f or several grains of Fe 43.8* 0.5percent, Cu 20.0t0.5 percent,S 20.3+0.5percent, total 84.1*4 per- cent. No other elementsdown to, and including, sodium could be de- tected;magnesium and aluminum, in particular, werelooked for, but not detected. The X-ray powder diffraction data (Table 1) of the Noril'sk material, which contained a minor amount of talnakhite (name used for the new copper-ironsulfi.de described by Cabri, 1967),can be indexedas valleriite, using the structure of Evans and Allmann (1968), except for a few re- flections. Some of these extraneousreflections were also reported b1' Genkin and VyaI'sov for the Noril'sk "valleriite." Sinceimpurities other than talnakhite were not detected with the microprobe, the extra re- flectionsmust be attributed to the structure of the mineral. Although the optical propertiesof the Noril'sk mineral are somewhal similar to other valleriites, the differencesare distinct enough to be a guide to its identification. Chamberlain and Delabio (1965), reported the optical propertiesof valleriite as dull bronze,similar to graphite in color, with extremebireflectance from cleamv bronze to purple at high magnifi.cation.Anisotropism was extreme,with colorsvarying from white to bronze.The Noril'sk material, however,is bluish gray, with a distinct bluish color in contrast to magnetite.Bireflectance is moderate,varying from a light grey to a dark bluish gral', in comparisonto the bronzecolor of valleriite. Anistropism is distinct, but less intense than that of val- Ieriite, with colorsvarying from light 1'ellowto reddish purple. Drscussrox The electron microprobe analysis of the so calied "valieriite'in the Noril'sk sampleyields a formula (cu6 ee5Fe1.6o15z). 1.472 [r'e(OH)r]. From the formula, the calculated OH-concentration is 15.8 percent 211+ MINITRALOGICAL NOTES which, combined with the microprobe analysis, gives a total of 99.9 percent. The X-ray powder pattern, indexed on Evans and Allmann's hexagonal cell vields cell dimensionso 3.778 and.c 34.147.A which are in close agreementwith that of normal valleriite oI a 3.792 and c 34.10 A. The Noril'sk mineral appearsto representthe end member of a seriesof "valleriite-type" minerals with the Mg-Al positions in the hl,droxidelayer occupiedb.v Fe. Acxxorvr,Blcrnrxr We r,vish to thank Dr J. Rucklidge, University of Toronto, who suggested the "val- leriite-type" formula from our microprobe analysis I{rlrnrNcns Caenr, L. I. 0967) A nerv copper-iron su1fide.Econ. Geol.62,9L0,925 exn R. J. Tnr,rr,r. (1966) New palladium minerals from Noril'sk, Western Siberia. Can. Mineral. 8, 541-550. Cu,trtrrnr..trm, J. A., eno R. N. Dnreero (1965) Mackinalvite and valleriite in the Muskox intrusion. Amer. Mineral 50,682 695. IivaNs, H. T., Jn., ano R. Ar.r.ulNN (1968) The crystal structure and crystal chemistr.v of valleriite. Z. Kristallogr., 127, 73-93. GnNr<rN, A. D., TnoNnva, N. V. aNo Znunnvr,rr, N. N. (1969) Pervaya nakhodka v rudakh sul'fida kaliya, zheleza i medi-djerfisherite. Geol. Ru.il. Mestorozhd. lf, (5), 57-64. eun L. N. Vver.'sov (1967) On valleriite i machinovite i usloviyakh ikh nakho- zhdeniya v rudakh.
Recommended publications
  • Mineral Processing
    Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19
    [Show full text]
  • Downloaded for Personal Non-Commercial Research Or Study, Without Prior Permission Or Charge
    MacArtney, Adrienne (2018) Atmosphere crust coupling and carbon sequestration on early Mars. PhD thesis. http://theses.gla.ac.uk/9006/ Copyright and moral rights for this work are retained by the author A copy can be downloaded for personal non-commercial research or study, without prior permission or charge This work cannot be reproduced or quoted extensively from without first obtaining permission in writing from the author The content must not be changed in any way or sold commercially in any format or medium without the formal permission of the author When referring to this work, full bibliographic details including the author, title, awarding institution and date of the thesis must be given Enlighten:Theses http://theses.gla.ac.uk/ [email protected] ATMOSPHERE - CRUST COUPLING AND CARBON SEQUESTRATION ON EARLY MARS By Adrienne MacArtney B.Sc. (Honours) Geosciences, Open University, 2013. Submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy at the UNIVERSITY OF GLASGOW 2018 © Adrienne MacArtney All rights reserved. The author herby grants to the University of Glasgow permission to reproduce and redistribute publicly paper and electronic copies of this thesis document in whole or in any part in any medium now known or hereafter created. Signature of Author: 16th January 2018 Abstract Evidence exists for great volumes of water on early Mars. Liquid surface water requires a much denser atmosphere than modern Mars possesses, probably predominantly composed of CO2. Such significant volumes of CO2 and water in the presence of basalt should have produced vast concentrations of carbonate minerals, yet little carbonate has been discovered thus far.
    [Show full text]
  • A Specific Gravity Index for Minerats
    A SPECIFICGRAVITY INDEX FOR MINERATS c. A. MURSKyI ern R. M. THOMPSON, Un'fuersityof Bri.ti,sh Col,umb,in,Voncouver, Canad,a This work was undertaken in order to provide a practical, and as far as possible,a complete list of specific gravities of minerals. An accurate speciflc cravity determination can usually be made quickly and this information when combined with other physical properties commonly leads to rapid mineral identification. Early complete but now outdated specific gravity lists are those of Miers given in his mineralogy textbook (1902),and Spencer(M,i,n. Mag.,2!, pp. 382-865,I}ZZ). A more recent list by Hurlbut (Dana's Manuatr of M,i,neral,ogy,LgE2) is incomplete and others are limited to rock forming minerals,Trdger (Tabel,l,enntr-optischen Best'i,mmungd,er geste,i,nsb.ildend,en M,ineral,e, 1952) and Morey (Encycto- ped,iaof Cherni,cal,Technol,ogy, Vol. 12, 19b4). In his mineral identification tables, smith (rd,entifi,cati,onand. qual,itatioe cherai,cal,anal,ys'i,s of mineral,s,second edition, New york, 19bB) groups minerals on the basis of specificgravity but in each of the twelve groups the minerals are listed in order of decreasinghardness. The present work should not be regarded as an index of all known minerals as the specificgravities of many minerals are unknown or known only approximately and are omitted from the current list. The list, in order of increasing specific gravity, includes all minerals without regard to other physical properties or to chemical composition. The designation I or II after the name indicates that the mineral falls in the classesof minerals describedin Dana Systemof M'ineralogyEdition 7, volume I (Native elements, sulphides, oxides, etc.) or II (Halides, carbonates, etc.) (L944 and 1951).
    [Show full text]
  • Shin-Skinner January 2018 Edition
    Page 1 The Shin-Skinner News Vol 57, No 1; January 2018 Che-Hanna Rock & Mineral Club, Inc. P.O. Box 142, Sayre PA 18840-0142 PURPOSE: The club was organized in 1962 in Sayre, PA OFFICERS to assemble for the purpose of studying and collecting rock, President: Bob McGuire [email protected] mineral, fossil, and shell specimens, and to develop skills in Vice-Pres: Ted Rieth [email protected] the lapidary arts. We are members of the Eastern Acting Secretary: JoAnn McGuire [email protected] Federation of Mineralogical & Lapidary Societies (EFMLS) Treasurer & member chair: Trish Benish and the American Federation of Mineralogical Societies [email protected] (AFMS). Immed. Past Pres. Inga Wells [email protected] DUES are payable to the treasurer BY January 1st of each year. After that date membership will be terminated. Make BOARD meetings are held at 6PM on odd-numbered checks payable to Che-Hanna Rock & Mineral Club, Inc. as months unless special meetings are called by the follows: $12.00 for Family; $8.00 for Subscribing Patron; president. $8.00 for Individual and Junior members (under age 17) not BOARD MEMBERS: covered by a family membership. Bruce Benish, Jeff Benish, Mary Walter MEETINGS are held at the Sayre High School (on Lockhart APPOINTED Street) at 7:00 PM in the cafeteria, the 2nd Wednesday Programs: Ted Rieth [email protected] each month, except JUNE, JULY, AUGUST, and Publicity: Hazel Remaley 570-888-7544 DECEMBER. Those meetings and events (and any [email protected] changes) will be announced in this newsletter, with location Editor: David Dick and schedule, as well as on our website [email protected] chehannarocks.com.
    [Show full text]
  • Mode of Occurrence and Mineralogy of Northern Khetri Copper Deposits, Jhunjhunu District, Rajasthan
    Natural Resources, 2018, 9, 389-403 http://www.scirp.org/journal/nr ISSN Online: 2158-7086 ISSN Print: 2158-706X Mode of Occurrence and Mineralogy of Northern Khetri Copper Deposits, Jhunjhunu District, Rajasthan Masood Ahmed*, Mohd Shaif, Farhat Naseem Siddiquie, Rajiullah Khan Department of Geology, Aligarh Muslim University, Aligarh, India How to cite this paper: Ahmed, M., Shaif, Abstract M., Siddiquie, F.N. and Khan, R. (2018) Mode of Occurrence and Mineralogy of Copper deposits in Khetri copper belt are hosted in the proterozoic sequence Northern Khetri Copper Deposits, Jhun- of rocks belonging to Ajabgarh group of Delhi supergroup situated in foot hill jhunu District, Rajasthan. Natural Re- zone of Aravalli mountain range North-West, India. Khetri copper belt is sources, 9, 389-403. https://doi.org/10.4236/nr.2018.912024 about 100 km long NE-SW trending metallogenic province, starting from Singhana in the north to Sangarava in the south. The study area is the north- Received: November 22, 2018 ern Khetri copper belt 190 km SW of Delhi, the capital city of India. In the Accepted: December 17, 2018 Published: December 20, 2018 present work an attempt has been made to determine the mode of occurrence and nature of mineralization with special emphasis on mineragraphic study Copyright © 2018 by authors and of copper ores. The ore bodies are found in the form of multiple lodes regio- Scientific Research Publishing Inc. nally but locally in the forms of veins, stringers, dissemination, sporadic, cav- This work is licensed under the Creative Commons Attribution International ity filling and replacement. Enriched mineralized zones are localized along License (CC BY 4.0).
    [Show full text]
  • Nickel Deposits of North America
    Nickel Deposits of North America By H. R. CORNWALL GEOLOGICAL SURVEY BULLETIN 1223 Geology, resources, and reserves of nickel sulfide and nickeliferous laterite deposits in 7 Provinces of Canada and 15 States of the United States UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1966 UNITED STATES DEPARTMENT OF THE INTERIOR STEWART L. UDALL, Secretary GEOLOGICAL SURVEY William T. Pecora, Director l!'irst printing 1966 Second printing 1967 For sale by the Superintendent of Documents, U.S. Government Printint Office Washintton, D.C. 20402- Price 25 cents (paper cover) CONTENTS Page Abstract---------------------------------------------------------- 1 Introduction __________________________ --.- _____________________ ---- 1 Types of deposits __________________________________________ ---- 2 Sulfide deposits------------------------------------------- 3 Nickeliferous laterite deposits _______ ------------------------ 4 Nickel minerals _____________________________ -----___ ---------- 4 Native nickel-iron _____________________________________ ---- 6 Sulfides-------------------------------------------------- 7 PenUandue___________________________________________ 7 Bravoite and violarite ______________________________ ---- 7 Vaesite----------------------------------------------- 8 8 Heazlewoodite_~illerite---------------------------------------------- __ __ _ _ __ __ __ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __ __ __ _ _ _____ 8 Linnaeite, polydymite, siegenite, and violarite_____________ 8 Other minerals ___ ------___________________________________
    [Show full text]
  • The Carbonatite-Hosted Apatite Deposit of Jacupiranga, SE Brazil: Styles of Mineralization, Ore Characterization and Association with Mineral Processing
    Scholars' Mine Masters Theses Student Theses and Dissertations Spring 2008 The carbonatite-hosted apatite deposit of Jacupiranga, SE Brazil: styles of mineralization, ore characterization and association with mineral processing Paula Regina Alves Follow this and additional works at: https://scholarsmine.mst.edu/masters_theses Part of the Geology Commons, and the Geophysics and Seismology Commons Department: Recommended Citation Alves, Paula Regina, "The carbonatite-hosted apatite deposit of Jacupiranga, SE Brazil: styles of mineralization, ore characterization and association with mineral processing" (2008). Masters Theses. 6723. https://scholarsmine.mst.edu/masters_theses/6723 This thesis is brought to you by Scholars' Mine, a service of the Missouri S&T Library and Learning Resources. This work is protected by U. S. Copyright Law. Unauthorized use including reproduction for redistribution requires the permission of the copyright holder. For more information, please contact [email protected]. i THE CARBONATITE-HOSTED APATITE DEPOSIT OF JACUPIRANGA, SE BRAZIL: STYLES OF MINERALIZATION, ORE CHARACTERIZATION, AND ASSOCIATION WITH MINERAL PROCESSING by PAULA REGINA ALVES A THESIS Presented to the Faculty of the Graduate School of the MISSOURI UNIVERSITY OF SCIENCE AND TECHNOLOGY In Partial Fulfillment of the Requirements for the Degree MASTER OF SCIENCE IN GEOLOGY 2008 Approved by R. D. Hagni, Advisor J. P. Hogan F. S. Miller ii iii ABSTRACT The carbonatite-hosted apatite deposit of Jacupiranga is located in southeastern Brazil. The major styles of apatite mineralization are veins or veinlets, small pods or patches, disseminated apatite, and massive aggregates (locally). The concentration of apatite involves grinding of the carbonatite, removal of magnetite with a magnet drum, size classification with cyclones, and flotation to suppress carbonates and collect apatite.
    [Show full text]
  • Orickite and Coyoteite, Two New Sulfide Minerals from Coyote Peak, Humboldt County, California
    American Mineralogist, Volume 68, pages 245-254, 1983 Orickite and coyoteite, two new sulfide minerals from Coyote Peak, Humboldt County, California RICHARD C. ERD AND GERALD K. CZAMANSKE U. S. Geological Survey Menlo Park, California 94025 Abstract Orickite and coyoteite occur with rare alkali iron sulfides in a mafic alkalic diatreme near Orick, Humboldt County, California. Both minerals are very rare, and only a few milligrams of each have been found. Orickite, NaxKyCuo.9sFe1.06Sz.zHzO (x,y < 0.03, z < 0.5), is hexagonal; a = 3.695, c = 6.16A (both :to.olA); D = 4.212 g cm-3 for Z = 4. The six strongest lines in the X-ray diffraction powder pattern are [d in A, I, (khl): 3.08, 100, (002); 3.20 90, (100); 2.84, 60, (101); 1.73, 55, (103); 1.583, 30, (112); 2.20, 15, (102). The mineral is brass yellow and opaque, weakly pleochroic, but strongly anisotropic (from grayish brown to grayish blue) in reflected light. Orickite is compositionally near iron-rich chalcopyrite, but the mineral may be related to synthetic chalcogenides having ajistorted wurtzite-(2H) structure. Coyoteite, NaFe3Ss'2HzO, is triclinic, PI or PI; a = 7.409(8), b = 9.881(6), c = 6.441(3)A, a = 100°25(3)', f3 = 104°37(5)', 81°29(5)'; D = 2.879 g cm-3 for Z = 2. The six 'Y = strongest lines in the powder patter~ are: 5.12,100,(111); 7.13,90,(100); 3.028,80,(220); 3.080,70,(002); 9.6,60,(010); 5.60,60,(011).
    [Show full text]
  • List of Mineral Symbols
    THE CANADIAN MINERALOGIST LIST OF SYMBOLS FOR ROCK- AND ORE-FORMING MINERALS (January 1, 2021) ____________________________________________________________________________________________________________ Ac acanthite Ado andorite Asp aspidolite Btr berthierite Act actinolite Adr andradite Ast astrophyllite Brl beryl Ae aegirine Ang angelaite At atokite Bll beryllonite AeAu aegirine-augite Agl anglesite Au gold Brz berzelianite Aen aenigmatite Anh anhydrite Aul augelite Bet betafite Aes aeschynite-(Y) Ani anilite Aug augite Bkh betekhtinite Aik aikinite Ank ankerite Aur auricupride Bdt beudantite Akg akaganeite Ann annite Aus aurostibite Beu beusite Ak åkermanite An anorthite Aut autunite Bch bicchulite Ala alabandite Anr anorthoclase Aw awaruite Bt biotite* Ab albite Atg antigorite Axn axinite-(Mn) Bsm bismite Alg algodonite Sb antimony Azu azurite Bi bismuth All allactite Ath anthophyllite Bdl baddeleyite Bmt bismuthinite Aln allanite Ap apatite* Bns banalsite Bod bohdanowiczite Alo alloclasite Arg aragonite Bbs barbosalite Bhm böhmite Ald alluaudite Ara aramayoite Brr barrerite Bor boralsilite Alm almandine Arf arfvedsonite Brs barroisite Bn bornite Alr almarudite Ard argentodufrénoysite Blt barylite Bou boulangerite Als alstonite Apn argentopentlandite Bsl barysilite Bnn bournonite Alt altaite Arp argentopyrite Brt baryte, barite Bow bowieite Aln alunite Agt argutite Bcl barytocalcite Brg braggite Alu alunogen Agy argyrodite Bss bassanite Brn brannerite Amb amblygonite Arm armangite Bsn bastnäsite Bra brannockite Ams amesite As arsenic
    [Show full text]
  • Valleriite 4(Fe, Cu)S • 3(Mg, Al)(OH)2 C 2001-2005 Mineral Data Publishing, Version 1
    Valleriite 4(Fe, Cu)S • 3(Mg, Al)(OH)2 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal Point Group: 32/m or 3m. Massive, as nodules, to 5 mm; also in tiny splinters, very thin flakes, and thin crusts. Physical Properties: Cleavage: On {0001}, excellent. Hardness = < 1, less than graphite. VHN = n.d. D(meas.) = 3.14 D(calc.) = 3.21 Optical Properties: Opaque. Color: Bronze-yellow, resembling pyrrhotite. Luster: Metallic to submetallic. Pleochroism: Strong; pale yellow to deep brown. Anisotropism: Strong; golden yellow. R1–R2: (400) 10.5–11.1, (420) 10.8–11.3, (440) 10.7–12.7, (460) 10.6–14.2, (480) 10.5–15.8, (500) 10.5–17.3, (520) 10.3–18.8, (540) 10.3–20.1, (560) 10.3–21.3, (580) 10.2–22.4, (600) 10.3–23.4, (620) 10.3–24.4, (640) 10.3–25.1, (660) 10.4–25.8, (680) 10.3–26.4, (700) 10.3–26.9 Cell Data: Space Group: R3m or R3m. a = 64.46 c = 34.10 Z = [390] X-ray Powder Pattern: Loolekop, South Africa. 11.39 (100), 5.71 (100), 3.27 (60), 3.80 (50), 3.23 (50), 2.846 (50), 1.885 (50) Chemistry: (1) (2) (3) (1) (2) (3) Cu 17.7 17.6 19.8 CaO 0.3 1.7 1.3 Fe 26.3 21.2 20.0 K2O 0.3 S 22.5 21.4 21.6 Na2O 0.6 Al2O3 5.1 8.1 8.5 H2O 10.8 12.2 10.8 MgO 10.6 16.2 16.0 SiO2 + insol.
    [Show full text]
  • Mackinawite (Fe, Ni)1+Xs (X = 0 to 0.11) C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Tetragonal
    Mackinawite (Fe, Ni)1+xS (x = 0 to 0.11) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Tetragonal. Point Group: 4/m 2/m 2/m. As well-formed thin tabular crystals, to 1 mm; massive, fine-feathery. Physical Properties: Cleavage: Very good on {001}. Hardness = Soft. VHN = 63–89 (15 g load). D(meas.) = n.d. D(calc.) = 4.30 Optical Properties: Opaque. Color: Bronzy. Streak: Black. Luster: Metallic. Pleochroism: Strong. Anisotropism: Extreme. R1–R2: (400) 17.7–25.7, (420) 17.0–28.0, (440) 16.4–30.2, (460) 16.2–32.2, (480) 16.1–34.4, (500) 16.0–36.5, (520) 16.1–38.4, (540) 16.1–40.0, (560) 16.3–41.4, (580) 16.5–42.5, (600) 16.7–43.3, (620) 17.0–43.9, (640) 17.2–44.3, (660) 17.4–44.5, (680) 17.5–44.6, (700) 17.7–44.6 Cell Data: Space Group: P 4/nmm. a = 3.6735(4) c = 5.0328(7) Z = 2 X-ray Powder Pattern: Mackinaw mine, Washington, USA. 5.03 (100), 2.31 (90), 1.809 (80), 2.96 (70), 1.838 (50), 1.729 (50), 1.055 (40) Chemistry: (1) (2) (3) (1) (2) (3) Fe 63.0 58.8 54.9 Ni 3.1 3.8 8.8 Cu 2.0 0.1 S 34.0 35.9 35.8 Co 0.4 Total 100.1 100.5 100.0 (1) Mackinaw mine, Washington, USA; by electron microprobe, corresponding to (Fe1.06Ni0.05)Σ=1.11S1.00.
    [Show full text]
  • AND ORE-FORMING MINERALS (December 30, 2019) ______
    THE CANADIAN MINERALOGIST LIST OF SYMBOLS FOR ROCK- AND ORE-FORMING MINERALS (December 30, 2019) ____________________________________________________________________________________________________________ Ac acanthite Adr andradite Ast astrophyllite Brl beryl Act actinolite Ang angelaite At atokite Bll beryllonite Ae aegirine Agl anglesite Au gold Brz berzelianite Aen aenigmatite Anh anhydrite Aul augelite Bet betafite Aes aeschynite-(Y) Ani anilite Aug augite Bkh betekhtinite Aik aikinite Ank ankerite Aur auricupride Bdt beudantite Akg akaganeite Ann annite Aus aurostibite Beu beusite Ak åkermanite An anorthite Aut autunite Bch bicchulite Ala alabandite Anr anorthoclase Aw awaruite Bt biotite* Ab albite Atg antigorite Axn axinite-(Mn) Bsm bismite Alg algodonite Sb antimony Azu azurite Bi bismuth All allactite Ath anthophyllite Bdl baddeleyite Bmt bismuthinite Aln allanite Ap apatite* Bns banalsite Bod bohdanowiczite Alo alloclasite Arg aragonite Bbs barbosalite Bhm böhmite Ald alluaudite Ara aramayoite Brr barrerite Bor boralsilite Alm almandine Arf arfvedsonite Brs barroisite Bn bornite Alr almarudite Ard argentodufrénoysite Blt barylite Bou boulangerite Als alstonite Apn argentopentlandite Bsl barysilite Bnn bournonite Alt altaite Arp argentopyrite Brt baryte, barite Bow bowieite Aln alunite Agt argutite Bcl barytocalcite Brg braggite Alu alunogen Agy argyrodite Bss bassanite Brn brannerite Amb amblygonite Arm armangite Bsn bastnäsite Bra brannockite Ams amesite As arsenic Bau baumstarkite Bnt braunite Amp amphibole* Ass arseniosiderite
    [Show full text]